Microdomain structure in polylactide-block-poly(ethylene oxide) copolymer films

被引:67
作者
Kubies, D [1 ]
Rypácek, F [1 ]
Kovárová, J [1 ]
Lednicky, F [1 ]
机构
[1] Acad Sci Czech Republ, Inst Macromol Chem, CR-16206 Prague 6, Czech Republic
关键词
tissue engineering; polylactide; poly(ethylene oxide); polylactide-block-poly(ethylene oxide)-block-polylactide; surface microdomains; microphase separation;
D O I
10.1016/S0142-9612(99)00219-7
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Structured surface is an important property of polymer biomaterials for tissue engineering, for its capacity to expose domains with different surface energy and functional groups. For this purpose, amphiphilic A-B-A block copolymers with polylactide (PLA) as A blocks and poly(ethylene oxide) (PEO 3, (M) over bar(n) = 3090; PEO6, (M) over bar(n) = 6110) as B block were synthesized by ring-opening polymerization of either L-lactide (L-LA) or DL-lactide (DL-LA), using poly(ethylene glycol)s as macroinitiators and tin(II) octanoate (Sn(Oct)(2)) as a catalyst. Differential scanning calorimetry (DSC) and electron microscopy were used to study the phase separation of the hydrophobic (PLA) and hydrophilic (PEO) segments in films made of the copolymers and their blends with high-molecular-weight PLA homopolymers. Hydrophilic (PEO) and hydrophobic (PLA) domains were formed at the polymer him surface due to the separation of phases. The phase separation was affected by the copolymer composition and the stereoregularity of PLA blocks in the copolymers. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:529 / 536
页数:8
相关论文
共 16 条
[1]   CELL-SEEDING AND IN-VITRO BIOCOMPATIBILITY EVALUATION OF POLYMERIC MATRICES OF PEO PBT COPOLYMERS AND PLLA [J].
BEUMER, GJ ;
VANBLITTERSWIJK, CA ;
BAKKER, D ;
PONEC, M .
BIOMATERIALS, 1993, 14 (08) :598-604
[2]  
CERRAI P, 1993, MAKROMOL CHEM-RAPID, V14, P529
[3]   BIODEGRADABLE POLYMER SCAFFOLDS FOR TISSUE ENGINEERING [J].
FREED, LE ;
VUNJAKNOVAKOVIC, G ;
BIRON, RJ ;
EAGLES, DB ;
LESNOY, DC ;
BARLOW, SK ;
LANGER, R .
BIO-TECHNOLOGY, 1994, 12 (07) :689-693
[4]  
Fujisato T, 1996, MACROMOL SYMP, V103, P73
[5]   LABORATORY SYNTHESIS OF POLYETHYLENE-GLYCOL DERIVATIVES [J].
HARRIS, JM .
JOURNAL OF MACROMOLECULAR SCIENCE-REVIEWS IN MACROMOLECULAR CHEMISTRY AND PHYSICS, 1985, C25 (03) :325-373
[6]  
KRICHELDORF HR, 1993, MAKROMOL CHEM, V194, P715
[7]  
KULKARNI R K, 1971, Journal of Biomedical Materials Research, V5, P169, DOI 10.1002/jbm.820050305
[8]   Synthesis, characterization, and hydrolytic degradation of PLA/PEO/PLA triblock copolymers with long poly(L-lactic acid) blocks [J].
Li, SM ;
Rashkov, I ;
Espartero, JL ;
Manolova, N ;
Vert, M .
MACROMOLECULES, 1996, 29 (01) :57-62
[9]   AN RGD SPACING OF 440NM IS SUFFICIENT FOR INTEGRIN ALPHA-V-BETA-3-MEDIATED FIBROBLAST SPREADING AND 140NM FOR FOCAL CONTACT AND STRESS FIBER FORMATION [J].
MASSIA, SP ;
HUBBELL, JA .
JOURNAL OF CELL BIOLOGY, 1991, 114 (05) :1089-1100
[10]   PREPARATION OF POLY(GLYCOLIC ACID) BONDED FIBER STRUCTURES FOR CELL ATTACHMENT AND TRANSPLANTATION [J].
MIKOS, AG ;
BAO, Y ;
CIMA, LG ;
INGBER, DE ;
VACANTI, JP ;
LANGER, R .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1993, 27 (02) :183-189